rs532190594

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs532190594(C;T)

Make rs532190594(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108140107

Gene

ACAT1

is a	snp
is	mentioned by
dbSNP	rs532190594
dbSNP (classic)	rs532190594
ClinGen	rs532190594
ebi	rs532190594
HLI	rs532190594
Exac	rs532190594
Gnomad	rs532190594
Varsome	rs532190594
LitVar	rs532190594
Map	rs532190594
PheGenI	rs532190594
Biobank	rs532190594
1000 genomes	rs532190594
hgdp	rs532190594
ensembl	rs532190594
geneview	rs532190594
scholar	rs532190594
google	rs532190594
pharmgkb	rs532190594
gwascentral	rs532190594
openSNP	rs532190594
23andMe	rs532190594
SNPshot	rs532190594
SNPdbe	rs532190594
MSV3d	rs532190594
GWAS Ctlg	rs532190594

Max Magnitude

0

ClinVar
Risk	rs532190594(T;T)
Alt	rs532190594(T;T)
Reference	Rs532190594(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ACAT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.108010834C>T
CLNSRC
CLNACC	RCV000434420.1,